Canonical Allele Identifier: CA377458826
Gene: BMPR1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2153565
ClinVar RCV Id: RCV003085730

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86917316A>C , CM000672.2:g.86917316A>C GRCh38
NC_000010.10:g.88677073A>C , CM000672.1:g.88677073A>C GRCh37
NC_000010.9:g.88667053A>C NCBI36
NG_009362.1:g.165678A>C , LRG_298:g.165678A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000480152.3:c.858A>C ENSP00000483569.2:p.Glu286Asp
ENST00000635816.2:c.858A>C ENSP00000489707.1:p.Glu286Asp
ENST00000636056.2:c.858A>C ENSP00000490273.1:p.Glu286Asp
ENST00000372037.8:c.858A>C MANE Select ENSP00000361107.2:p.Glu286Asp
ENST00000635816.1:c.858A>C ENSP00000489707.1:p.Glu286Asp
ENST00000636056.1:c.858A>C ENSP00000490273.1:p.Glu286Asp
ENST00000638429.1:c.858A>C ENSP00000492290.1:p.Glu286Asp
ENST00000372037.7:c.858A>C ENSP00000361107.1:p.Glu286Asp
NM_004329.2:c.858A>C , LRG_298t1:c.858A>C NP_004320.2:p.Glu286Asp
XM_011540103.1:c.858A>C XP_011538405.1:p.Glu286Asp
XM_011540104.1:c.858A>C XP_011538406.1:p.Glu286Asp
XM_011540103.2:c.858A>C XP_011538405.1:p.Glu286Asp
XM_011540104.2:c.858A>C XP_011538406.1:p.Glu286Asp
NM_004329.3:c.858A>C MANE Select NP_004320.2:p.Glu286Asp